CARDINAL HEALTH SCV44CWSLDRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10888439542554), received between Dec 19, 2019 and Dec 19, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Contamination /Decontamination Problem” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionDec 19, 2019Contamination /Decontamination Problem

  THE CUSTOMER REPORTED THAT LINT FROM LAP SPONGES, LS1818PSA, FROM THE CV PACK, SCV44CWSLD, WAS FALLING INTO THE VESSELS DURING CV CASES. LINT WAS FOUND IN OR AROUND CAVITIES, AND BARRIER BETWEEN INSTRUMENTS AND THE PATIENT. THERE WAS A DELAY, BUT NO INJURY TO THE PATIENT. MDR BEING REPORTED BASED ON POTENTIAL RISK TO THE PATIENT.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9492507 ↗